Monday, June 16, 2014

An short update on cancer ward

A lot has happened health wise since my last entry on here, so much I don't know where to start. The main thing is that my chemo has come to an end. When I arrived at hospital for my seventh and final round of chemo to commence on 5 th June the doctors decided that they could not let me home as my white cell count was so low and especially because I was dehydrated yet again. I was kept in hospital for four nights until the Monday. 

My consultant, Dr McLean came to see me a few times while I was there and the upshot was that she decided that I should not have anymore chemo, as she feared it would do permanent damage to my poor organs , especially my kidneys. However she assures me that this should have no impact on the final outcome of my treatment. The plan still remains a complete cure. 

It's a huge relief to know that I will not have any more chemo to cope with. I feel mentally and psychologically better as a result, though a bit disappointed the way it all happened. I would have preferred to get through the last cycle and not to have it cancelled, but I've now accepted that decision and getting on with things. I will see Dr McLean again on July but won't know whether or not all that chemo was worth it, until I have my scan in November. It seems a long time to wait but once again I shall be patient. Patience not being my greatest virtue. Goodness knows where I've found the patience to cope since being diagnosed with cancer over a year ago. Last May in fact. Mind you my surgeon did warn me to set aside at least a year for the whole procees to be completed. 

I saw Mr Speake,my surgeon again last week. He hopes to be able to operate to reverse my stoma later this summer and maybe as early as July, though I need a contrast scan on the operation area before then and somehow I think he is being optimistic. 

That's all for now folks. I hope to be able to spend less time writing about my health and concentrate on other things, now that I'm not actually undergoing any treatment. First stop will be Blackford Pond. 

Wednesday, June 04, 2014

A Motto for Life

I should have started my sixth and final cycle of chemo on Monday 2 June but my neutrophils let me down again. Very low this time. And there was me thinking that after my stay in hospital I would be a lot fitter and ready for my final fling with the chemo. But no such luck; the nurses said why change now? 

For the scientists among you a neutrophil is a phagocytic white blood cell having a lobulate nucleus and neutrophil granules in the cytoplasm and the little buggers have given me much grief over the last six months which is strange as I never knew I had them before.

The plan now is to go back tomorrow, Thursday, to try again. But mustn't raise my hopes as nurses on Ward One thought my neutrophils were on a downward trajectory so may not have recovered by tomorrow. I won't be having any more intravenous chemo, just the tablets, as Dr McLean does not think my poor body can cope with much more chemo. So fingers crossed for tomorrow. 

It's late at night now and need to get my beauty sleep for tomorrow which is also Maggie's Centre support group summer lunch, which I hope to be able to attend, with the co-operation of the nurses on Ward One. 

I will finish tonight with some quotes from Maya Angelou who died a few days ago, sadly. She was a fine writer, poet and performer. She wrote: 

" You may write me down in history
   With your bitter twisted lies,
   You may trod me in the very dirt 
   But still, like dust, I'll rise." 

" You may not control all the events that happen to you , but you can decide not to be reduced by 
   them." 

Which I have adopted as my motto for life. So neutrophils will not be allowed to control my life.